Over-the-counter drug · ANDA
Ana-Dent PAIN RELIEF (naproxen sodium) NDC 27854-701
Naproxen sodium 220 mg/1 · Tablet, Film coated · Oral · Belmora LLC
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 27854-701-01 | 27854070101 | 1 BOTTLE in 1 CARTON (27854-701-01) / 24 TABLET, FILM COATED in 1 BOTTLEMarketed from May 15, 2020 |
How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- Ana-Dent PAIN RELIEF
- Generic name (nonproprietary)
- naproxen sodium
- Active ingredients
- Naproxen sodium — 220 mg/1
- Dosage form
- Tablet, Film coated
- Route
- Oral
- Labeler
- Belmora LLC
- Product type
- Over-the-counter drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 205497
- Marketing start
- Listing expires
- Other FDA classes
- Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
- Identifiers
- Product ID 27854-701_5ac02446-13da-43d5-9647-fe469294acecSPL ID 5ac02446-13da-43d5-9647-fe469294acecSPL set ID 04721306-2850-4e0a-9dd9-7cabb575f3c7RxCUI 849574UNII 9TN87S3A3C
- Pharmacologic class
- Nonsteroidal Anti-inflammatory Drug
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N427854070101followed by a unit qualifier and the quantityPackage 27854-0701-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Label details couldn’t be retrieved right now. Open the label on DailyMed.
Other NDCs under ANDA 205497
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Naproxen Sodium HEADACHE PAINnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Aurohealth LLC | 58602-737 |
| Naproxen Sodium HEADACHE PAINnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Aurohealth LLC | 58602-735 |
| Naproxen Sodium BACK AND MUSCLE PAINnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Aurohealth LLC | 58602-736 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Aurohealth LLC | 58602-738 |
| Naproxen Sodium BACK AND MUSCLE PAINnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Aurohealth LLC | 58602-739 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Aurohealth LLC | 58602-819 |
| Amazon Basic Care Naproxen Sodiumnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Amazon.com Services LLC | 72288-366 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Aurohealth LLC | 58602-845 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | WALMART INC. | 79903-232 |
| Flanax Pain Reliever/Fever Reducernaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Belmora LLC | 27854-700 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | WALMART INC. | 79903-231 |